Heyduk E, Heyduk T
Edward A. Doisy Department of Biochemistry and Molecular Biology, St. Louis University Medical School, Missouri 63104, USA.
Anal Biochem. 1997 Jun 1;248(2):216-27. doi: 10.1006/abio.1997.2148.
Lanthanide chelates have recently been shown to be extremely promising luminescence probes for distance measurements in biomolecules using luminescence resonance energy transfer measurements [P. R. Selvin, T. M. Rana, and J. E. Hearst (1994) J. Am. Chem. Soc. 116, 6029-6030; P. R. Selvin, and J. E. Hearst (1994) Proc. Natl. Acad. Sci. USA 91, 10024-10028]. In this work we describe simple procedures for preparing highly fluorescent thiol-reactive europium chelates. These new compounds contain a uv-absorbing coumarin group which sensitizes europium emission, diethylenetriaminepentaacetic acid or triethylenetetraaminehexaacetic acid groups which provide europium chelating function, and a pyridyl disulfide group which allows specific modification of thiol groups. These reagents can be used to label proteins at Cys residues or synthetic oligonucleotides which contain thiol groups. Modification can be reversed easily by treatment with a reducing agent (dithiothreitol). Luminescence energy transfer between these new chelates and CY5 fluorochrome attached to the opposite ends of 15-bp double-stranded DNA was measured to test their usefulness for distance measurements in macromolecules. The distance measured between the chelate (donor) and CY5 (acceptor) was in the range expected for the length of 15-bp DNA. The stability of europium chelates and their conjugates with a protein, the precision of distance measurements using these chelates, possible errors due to intramolecular energy transfer, and the modulation of the R0 value with deuterium oxide were tested. The results obtained fully confirmed the great potential of these new probes for sensitive, simple, and precise distance measurements in biomolecules using luminescence resonance energy transfer.
最近研究表明,镧系螯合物是极具前景的发光探针,可用于通过发光共振能量转移测量法来测定生物分子中的距离[P. R. 塞尔文、T. M. 拉纳和J. E. 赫斯特(1994年)《美国化学会志》116卷,6029 - 6030页;P. R. 塞尔文和J. E. 赫斯特(1994年)《美国国家科学院院刊》91卷,10024 - 10028页]。在本研究中,我们描述了制备高荧光硫醇反应性铕螯合物的简单方法。这些新化合物含有一个能敏化铕发射的紫外吸收香豆素基团、提供铕螯合功能的二乙三胺五乙酸或三乙烯四胺六乙酸基团,以及一个可对硫醇基团进行特异性修饰的吡啶基二硫化物基团。这些试剂可用于在半胱氨酸残基处标记蛋白质或标记含有硫醇基团的合成寡核苷酸。用还原剂(二硫苏糖醇)处理可轻松逆转修饰。测量了这些新螯合物与连接在15碱基对双链DNA两端的CY5荧光染料之间的发光能量转移,以测试它们在大分子距离测量中的实用性。所测得的螯合物(供体)与CY5(受体)之间的距离在15碱基对DNA长度预期的范围内。测试了铕螯合物及其与蛋白质的缀合物的稳定性、使用这些螯合物进行距离测量的精度、分子内能量转移可能导致的误差以及氧化氘对R0值的调节。所获得的结果充分证实了这些新探针在利用发光共振能量转移对生物分子进行灵敏、简单且精确的距离测量方面具有巨大潜力。